Retrovirus gag protein p30 in the islets of non-obese diabetic mice: relevance for pathogenesis of diabetes mellitus

Diabetologia. 1992 Jul;35(7):614-8. doi: 10.1007/BF00400251.

Abstract

We investigated the presence of retroviral protein in the pancreatic islets of non-obese diabetic mice to prove that the virus-like particle observed specifically in the pancreatic Beta cell of these mice was retrovirus. Western blot analysis probed with anti-retrovirus antibody demonstrated the existence of retroviral gag (group specific antigen) protein p30 in the islets of female non-obese diabetic mice. Islets of non-obese diabetic mice which were treated with cyclophosphamide, known to accelerate the development of insulitis and diabetes mellitus, have shown both a significantly increased number of retrovirus-like particles (type C) and enhanced expression of gag protein p30, compared to those of mice not treated with cyclophosphamide. These results confirmed the presence of type C retrovirus in non-obese diabetic mouse Beta cells and suggest a role for retrovirus in the development of insulitis and diabetes in these mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cyclophosphamide / pharmacology
  • Diabetes Mellitus, Type 1 / etiology
  • Diabetes Mellitus, Type 1 / microbiology*
  • Diabetes Mellitus, Type 1 / pathology
  • Endoplasmic Reticulum / microbiology
  • Endoplasmic Reticulum / ultrastructure
  • Gene Products, gag / analysis*
  • Islets of Langerhans / drug effects
  • Islets of Langerhans / microbiology*
  • Islets of Langerhans / pathology
  • Mice
  • Mice, Inbred NOD
  • Retroviridae / genetics
  • Retroviridae / isolation & purification*

Substances

  • Gene Products, gag
  • Cyclophosphamide